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MODELING DOWN SYNDROME NEURAL PHENOTYPES WITH CHROMOSOMAL SILENCING |
| 1F30HD086975-01A1 |
CZERMINSKI, JAN |
NICHD |
2017 |
|
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FOLATE-P53 INTERACTIONS IN NEURAL TUBE DEFECTS |
| 1F30HD093288-01 |
LACHENAUER, ERICA ROSE |
NICHD |
2017 |
|
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CHEMICALLY MODIFIED PEPTIDE AGENTS FOR NEXT-GENERATION CONJUGATE THERAPIES TO TREAT DUCHENNE MUSCULAR DYSTROPHY |
| 1F30HD093358-01 |
FADZEN, COLIN MACLAINE |
NICHD |
2017 |
|
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IDENTIFYING RISK MARKERS FOR AUTISM SPECTRUM DISORDERS IN EARLY INFANCY: A MULTIMODAL APPROACH |
| 1F31HD090937-01A1 |
TSANG, TAWNY |
NICHD |
2017 |
|
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DYRK1A DYSREGULATION IN TRISOMY 21 AND DYRK1A HAPLOINSUFFICIENCY LEAD TO MIDFACE HYPOPLASIA |
| 1F32HD091977-01 |
WAHL, STACEY ELIZABETH |
NICHD |
2017 |
|
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FUNCTION OF SLACK POTASSIUM CHANNELS IN EARLY ONSET EPILEPSY AND INTELLECTUAL DISABILITIES |
| 1F32HD093292-01 |
ALI, SYED RYDWAN |
NICHD |
2017 |
|
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THE ROLE OF INHIBITORY NEURONS IN MICROCEPHALY AND SEIZURE CAUSED BY ASPARAGINE SYNTHETASE (ASNS) DEFICIENCY |
| 1F32HD094625-01A1 |
YAO, XIAODI |
NICHD |
2017 |
|
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THE NEURAL FUNCTIONS OF RAI1, THE CAUSAL GENE FOR SMITH-MAGENIS SYNDROME |
| 1K99HD092545-01 |
HUANG, WEI-HSIANG |
NICHD |
2017 |
|
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CENTRAL & PERIPHERAL BLOOD FLOW REGULATION IN INDIVIDUALS WITH DOWN SYNDROME |
| 1K99HD092606-01 |
HILGENKAMP, THESSA |
NICHD |
2017 |
|
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SPEECH RHYTHM ACQUISITION |
| 1R01HD087452-01A1 |
REDFORD, MELISSA A |
NICHD |
2017 |
